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The Psychiatric Quarterly|September 5, 2020
The Attitude towards Preventive Measures and Knowledge of COVID-19 Inpatients with Severe Mental Illness in Economically Underdeveloped Areas of ChinaJu-Hong Zhu, Wen Li, Xiao-Ning Huo, et al.Biochemistry|June 5, 2007
Probing the binding site of the A1 adenosine receptor reengineered for orthogonal recognition by tailored nucleosidesKrishnan K Palaniappan, Zhan-Guo Gao, Andrei A Ivanov, et al.European Journal of Medicinal Chemistry|November 30, 2021
A3 adenosine receptor agonists containing dopamine moieties for enhanced interspecies affinityDilip K Tosh, Veronica Salmaso, Ryan G Campbell, et al.Bioorganic & Medicinal Chemistry|April 21, 2009
Structure-activity relationships of truncated adenosine derivatives as highly potent and selective human A3 adenosine receptor antagonistsShantanu Pal, Won Jun Choi, Seung Ah Choe, et al.Scientific Reports|May 5, 2016
Gold@silver bimetal nanoparticles/pyramidal silicon 3D substrate with high reproducibility for high-performance SERSChao Zhang, Shou Zhen Jiang, Cheng Yang, et al.ACS Omega|November 10, 2018
Repurposing of a Nucleoside Scaffold from Adenosine Receptor Agonists to Opioid Receptor AntagonistsDilip K Tosh, Antonella Ciancetta, Philip Mannes, et al.Journal of Medicinal Chemistry|August 22, 2003
N6-substituted D-4'-thioadenosine-5'-methyluronamides: potent and selective agonists at the human A3 adenosine receptorLak Shin Jeong, Dong Zhe Jin, Hea Ok Kim, et al.Journal of Medicinal Chemistry|April 10, 2020
Truncated (N)-Methanocarba Nucleosides as Partial Agonists at Mouse and Human A3 Adenosine Receptors: Affinity Enhancement by N6-(2-Phenylethyl) SubstitutionDilip K Tosh, Veronica Salmaso, Harsha Rao, et al.Bioorganic & Medicinal Chemistry Letters|February 8, 2008
Structure-activity relationships of 2-chloro-N6-substituted-4'-thioadenosine-5'-N,N-dialkyluronamides as human A3 adenosine receptor antagonistsLak Shin Jeong, Hyuk Woo Lee, Hea Ok Kim, et al.European Journal of Medicinal Chemistry|June 25, 2021
Synthesis and evaluation of adenosine derivatives as A1, A2A, A2B and A3 adenosine receptor ligands containing boron clusters as phenyl isosteres and selective A3 agonistsKatarzyna Bednarska-Szczepaniak, Adam Mieczkowski, Aleksandra Kierozalska, et al.Pageof 37